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M Cruts

Showing results (61-70 of 80) with videos related to

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American Journal of Human Genetics|January 23, 1999
The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer diseaseB Dermaut, M Cruts, A J Slooter, et al.
Stroke|September 8, 2001
Apolipoprotein E and carotid artery atherosclerosis: the Rotterdam studyA J Slooter, M L Bots, L M Havekes, et al.
Neurology|September 12, 2000
The alpha2-macroglobulin gene in AD: a population-based study and meta-analysisM N Koster, B Dermaut, M Cruts, et al.
Human Molecular Genetics|February 28, 1998
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer diseaseM Cruts, C M van Duijn, H Backhovens, et al.
Neurology|February 4, 2010
Genetic contribution of FUS to frontotemporal lobar degenerationT Van Langenhove, J van der Zee, K Sleegers, et al.
Human Genetics|August 14, 2001
The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's diseaseJ Theuns, L Feuk, B Dermaut, et al.
Brain : a Journal of Neurology|May 8, 2004
Familial clustering and genetic risk for dementia in a genetically isolated Dutch populationK Sleegers, G Roks, J Theuns, et al.
Human Molecular Genetics|November 7, 2000
Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's diseaseS Kumar-Singh, C De Jonghe, M Cruts, et al.
Human Mutation|August 19, 2006
Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragmentJ Theuns, E Marjaux, M Vandenbulcke, et al.
Genome Research|November 24, 1999
A high-resolution physical map of human chromosome 21p using yeast artificial chromosomesS Y Wang, M Cruts, J Del-Favero, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|January 23, 1999
The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer diseaseB Dermaut, M Cruts, A J Slooter, et al.
Stroke|September 8, 2001
Apolipoprotein E and carotid artery atherosclerosis: the Rotterdam studyA J Slooter, M L Bots, L M Havekes, et al.
Neurology|September 12, 2000
The alpha2-macroglobulin gene in AD: a population-based study and meta-analysisM N Koster, B Dermaut, M Cruts, et al.
Human Molecular Genetics|February 28, 1998
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer diseaseM Cruts, C M van Duijn, H Backhovens, et al.
Neurology|February 4, 2010
Genetic contribution of FUS to frontotemporal lobar degenerationT Van Langenhove, J van der Zee, K Sleegers, et al.
Human Genetics|August 14, 2001
The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's diseaseJ Theuns, L Feuk, B Dermaut, et al.
Brain : a Journal of Neurology|May 8, 2004
Familial clustering and genetic risk for dementia in a genetically isolated Dutch populationK Sleegers, G Roks, J Theuns, et al.
Human Molecular Genetics|November 7, 2000
Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's diseaseS Kumar-Singh, C De Jonghe, M Cruts, et al.
Human Mutation|August 19, 2006
Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragmentJ Theuns, E Marjaux, M Vandenbulcke, et al.
Genome Research|November 24, 1999
A high-resolution physical map of human chromosome 21p using yeast artificial chromosomesS Y Wang, M Cruts, J Del-Favero, et al.
Pageof 8